Pesquisa | SciELO

Resumo: Objetiva-se desvelar os motivos para hesitação vacinal de pais e/ou responsáveis de crianças e adolescentes para prevenção da COVID-19. Trata-se de um estudo descritivo, de abordagem qualitativa, que busca analisar as respostas da pergunta aberta “por que você não vai vacinar, não vacinou ou está na dúvida em vacinar as crianças e os adolescentes sob sua responsabilidade para prevenção da COVID-19?”. A pesquisa incluiu indivíduos adultos, brasileiros, residentes no país, responsáveis por crianças e adolescentes menores de 18 anos. A coleta de dados aconteceu de forma eletrônica entre os meses de novembro e dezembro de 2021. As respostas foram organizadas e processadas com suporte do software Iramuteq. O corpus textual desta pesquisa foi composto pela resposta de 1.896 participantes, constituído por 87% de hesitantes (1.650) e 13% (246) de pais que têm intenção de vacinar, mas que esboçaram algumas dúvidas e considerações a respeito da vacinação de crianças e adolescentes. São motivos pelos quais pais e/ou responsáveis não vacinaram ou estão na dúvida em vacinar as crianças e os adolescentes sob sua responsabilidade para prevenção da COVID-19: receio em razão de a vacina estar em fase experimental e medo das reações adversas e dos efeitos a longo prazo. Já os motivos para ausência de intenção de vacinar decorrem dos entendimentos dos participantes de que a COVID-19 em crianças não é grave, os riscos da vacinação são maiores do que os benefícios e o direito de escolha em não vacinar.

Resumen: El objetivo es revelar los motivos de la indecisión a las vacunas de padres y/o responsables de niños y adolescentes para la prevención de COVID-19. Se trata de un estudio descriptivo con enfoque cualitativo, que busca analizar las respuestas a la pregunta abierta “¿Por qué no va a vacunar o no vacunó o tiene dudas en vacunar a los niños y los adolescentes bajo su responsabilidad para la prevención del COVID-19?”. La investigación incluyó individuos adultos, brasileños, residentes en el país, responsables de niños y adolescentes menores de 18 años. La recolección de datos se realizó de forma electrónica entre los meses de noviembre y diciembre de 2021. Las respuestas se organizaron y procesaron con ayuda del software Iramuteq. El corpus textual de esta investigación fue compuesto por la respuesta de 1.896 participantes, siendo constituido por el 87% de indecisos (1.650) y el 13% (246) de padres que tienen la intención de vacunar, pero que esbozaron algunas dudas y consideraciones respecto a la vacunación de niños y adolescentes. Son motivos por los cuales los padres y/o responsables no vacunaron o están en duda en vacunar a los niños y adolescentes bajo su responsabilidad para prevención del COVID-19: temores con la vacunación en cuanto a la concepción de que la vacuna está en fase experimental, miedo a las reacciones adversas y los efectos a largo plazo. Los motivos de la ausencia de intención en vacunar se deben a que los participantes entienden que el COVID-19 en niños no es grave, que los riesgos de la vacunación son mayores que los beneficios y que tienen derecho a decidir no vacunarse.

Abstract: The objective is to unveil the reasons for vaccine hesitancy among parents and/or guardians of children and adolescents toward the prevention of COVID-19. This is a descriptive study, with a qualitative approach that seeks to analyze the answers to the open question “Why will you not vaccinate or have not vaccinated or are in doubt about vaccinating the children and adolescents under your responsibility, for the prevention of COVID-19?”. The research included adult individuals, Brazilians, living in the country, responsible for children and adolescents under 18 years of age. Data collection took place electronically in November and December 2021. The answers were organized and processed with the support of the software Iramuteq. The textual corpus of this research was composed of the response of 1,896 participants, consisting of 87% who were hesitant (1,650) and 13% (246) of parents who intend to vaccinate but who outlined some doubts and considerations about the vaccination of children and adolescents. These are reasons why parents and/or guardians have not vaccinated or are in doubt about vaccinating the children and adolescents under their responsibility for the prevention of COVID-19: fears about vaccination regarding the conception that the vaccine is in the experimental phase, fear of adverse reactions and long-term effects. The reasons for the lack of intention to vaccinate stem from the understanding of the participants that COVID-19 in children is not serious, the risks of vaccination are greater than the benefits, and the right of choice not to vaccinate.

https://doi.org/10.1590/0102-311xpt159122

Inquérito online sobre os motivos para hesitação vacinal contra a COVID-19 em crianças e adolescentes do Brasil
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Salvador, Pétala Tuani Candido de Oliveira

; Alves, Kisna Yasmin Andrade

; Carvalho, Katiuscia Roseli Silva de

; Nehab, Marcio Fernandes

; Camacho, Karla Gonçalves

; Reis, Adriana Teixeira

; Junqueira-Marinho, Maria de Fátima

; Abramov, Dimitri Marques

; Azevedo, Zina Maria Almeida de

; Salú, Margarida dos Santos

; Vasconcelos, Zilton Farias Meira de

; Gomes Junior, Saint Clair dos Santos

; da Silva Filho, Orli Carvalho

; Moore, Daniella Campelo Batalha Cox

Cadernos de Saúde Pública

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2023, Volume 39 Nº 10 elocation e00159122

Resumo: En Es Pt | Texto: En Es Pt | PDF: En | PDF: Es | PDF: Pt

https://doi.org/10.1590/0102-311xpt159122

Wound healing - A literature review
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Gonzalez, Ana Cristina de Oliveira

; Costa, Tila Fortuna

; Andrade, Zilton de Araújo

; Medrado, Alena Ribeiro Alves Peixoto

Anais Brasileiros de Dermatologia

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Out 2016, Volume 91 Nº 5 Páginas 614 - 620

Resumo: En | Texto: En | PDF: En

Abstract: Regeneration and tissue repair processes consist of a sequence of molecular and cellular events which occur after the onset of a tissue lesion in order to restore the damaged tissue. The exsudative, proliferative, and extracellular matrix remodeling phases are sequential events that occur through the integration of dynamic processes involving soluble mediators, blood cells, and parenchymal cells. Exsudative phenomena that take place after injury contribute to the development of tissue edema. The proliferative stage seeks to reduce the area of tissue injury by contracting myofibroblasts and fibroplasia. At this stage, angiogenesis and reepithelialization processes can still be observed. Endothelial cells are able to differentiate into mesenchymal components, and this difference appears to be finely orchestrated by a set of signaling proteins that have been studied in the literature. This pathway is known as Hedgehog. The purpose of this review is to describe the various cellular and molecular aspects involved in the skin healing process.

https://doi.org/10.1590/abd1806-4841.20164741 19925 downloads

The significance of the amoebocyte-producing organ in Biomphalaria glabrata
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Souza, Samaly dos Santos

; Andrade, Zilton Araújo

Memórias do Instituto Oswaldo Cruz

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Ago 2012, Volume 107 Nº 5 Páginas 598 - 603

Resumo: En | Texto: En | PDF: En

In molluscs, internal defence against microorganisms is performed by a single cell type, i.e., the haemocyte or amoebocyte. The origin of these cells in Biomphalaria glabrata was initially thought to be localised within the vasculo-connective tissue. More recently, origin from a single organ, termed the amoebocyte-producing organ (APO), has been postulated based on the occurrence of hyperplasia and mitoses during Schistosoma mansoni infection. The present investigation represents a histological, immuno-histochemical and ultra-structural study of the B. glabrata APO, whereby histological identification was facilitated by means of collecting epithelial basophilic cells. These cells were comprised of single-cell layers that cover a portion of the stroma, which contains many small, round cells and haemolymph sinuses, as well as a small area of the pericardial surface of the reno-pericardial region. On occasion, this epithelial component vaguely resembled the vertebrate juxtaglomerular apparatus, which reinforces its presumed relationship to the kidney. Both in normal and infected molluscs, mitoses were only occasionally found. The present quantitative studies failed to demonstrate the presence of APO cellular hyperplasia, either in normal or schistosome-infected B. glabrata. Conversely, several structural details from the APO region in B. glabrata were found to be consistent with the hypothesis that the APO is a filtration organ, i.e., it is more closely related to the kidney rather than the bone marrow, as has been suggested in the literature.

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Dynamics of Capillaria-hepatica-induced hepatic septal fibrosis in rats
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Gaban, Lidiane

; Ramos, Cleber Douglas Lucinio

; Barbosa Júnior, Aryon Almeida

; Souza, Márcia Maria de

; Andrade, Zilton de Araújo

Revista da Sociedade Brasileira de Medicina Tropical

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Dez 2010, Volume 43 Nº 6 Páginas 643 - 646

Resumo: Pt En | Texto: Pt En | PDF: Pt | PDF: En

INTRODUÇÃO: Um extenso material de patologia experimental arquivado em blocos de parafina, ilustrativo das diferentes fases da fibrose hepática septal, que 100% dos ratos desenvolvem em seguida uma infecção com o nematódeo Capillaria hepatica. MÉTODOS: O material foi sistematicamente estudado com métodos morfológicos e morfométricos, no sentido de se verificar o comportamento dos elementos celulares e matriciais durante a evolução da fibrose hepática septal ao longo de um período de um ano. RESULTADOS: Foi constatado que a fibrose septal se origina de vários espaços porta ao mesmo tempo, com proliferação vascular (angiogênese), multiplicação de células actino-positivas (pericitos, miofibroblastas) e progressivo depósito de colágeno. Ao fim dos 4-5 meses há uma involução regressiva de todos estes indícios morfológicos, mas com alguns septos persistindo bem evidentes até o fim de um ano. CONCLUSÕES: Além de ilustrar o papel fundamental desempenhado pela angiogênese, o modelo se mostrou adequado para futuros estudos funcionais relacionados com a indução, progressão e regressão da fibrose hepática.

INTRODUCTION: The pathogenesis of septal hepatic fibrosis, induced in rats by Capillaria hepatica infection, was studied with the aid of a large collection of stored paraffin blocks, representative of the different evolutive phases of fibrosis which appeared in 100% of infected rats. METHODS: Studies were conducted involving histology, immunohistochemistry, immunofluorescence and morphometric methods, in order to observe the dynamic behavior of the cellular and matrix components of fibrosis, over a one year period of evolution. RESULTS: Observation verified that septal fibrosis originates from several portal spaces simultaneously. Its origin and progression involve blood vessel proliferation (angiogenesis), multiplication of actin-positive cells (pericytes and myofibroblasts) and progressive collagen deposition. By the end of 4-5 months, a progressive decrease in all these components was observed, when signs of regression of septal fibrosis became more evident over time. CONCLUSIONS: Besides indicating the fundamental role played by angiogenesis in the pathogenesis of fibrosis, these morphological data concerning the dynamics of this C. hepatica experimental model proved to be adequate for future investigations regarding the functional aspects of fibrosis induction, progression and regression.

1865 downloads Citado 2 vezes em SciELO

Capillaria hepatica-induced septal fibrosis in rats: a contribution to the study of liver fibrogenesis
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Barbosa, Valter Lucas Chaves

; Andrade, Zilton de Araújo

Revista da Sociedade Brasileira de Medicina Tropical

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Out 2010, Volume 43 Nº 5 Páginas 504 - 507

Resumo: Pt En | Texto: Pt En | PDF: Pt | PDF: En

INTRODUÇÃO: A fibrose septal do fígado se desenvolve regularmente em ratos infectados pelo nematódeo Capillaria hepatica. O tratamento curativo da infecção, feito antes do 15º dia da infecção, mas não mais tarde, impediu o aparecimento da fibrose septal. O presente trabalho procura verificar qual o estado do parasitismo aos 15 dias da infecção, crucial para patogenia da fibrose septal. MÉTODOS: Ratos foram infectados por via digestiva com 600 ovos embrionados de C. hepatica e tratados com Ivermectina e mebendazol, em grupos separados, aos 10, 12, 15, 17 ou 20 dias após a infecção. O animal de cada grupo e seus respectivos controles foram mortos e examinados aos 40 dias após o fim do tratamento. RESULTADOS: Os achados aos 15 dias da infecção mostraram a maturação completa da parasitose, com presença de ovos e vermes, circundados por reação necro-inflamatória, mas ainda sem fibrose septal. Daí por diante, a fibrose septal se fez presente. CONCLUSÕES: Como os vermes morrem espontaneamente após o 15º dia da infecção, não apenas a origem, mas o posterior crescimento e a manutenção da fibrose septal dependem da presença dos ovos acumulados no fígado, os quais são os únicos elementos parasitários presentes após o 15º dia da infecção por C. hepatica no rato.

INTRODUCTION: Septal fibrosis of the liver regularly develops in rats infected with the nematode Capillaria hepatica. Curative treatment of the infection prevents the development of septal fibrosis when intervention occurs up to postinfection day (PID) 15, but not later. The present investigation aimed to demonstrate which parasitic factors are present when the process of septal fibrosis can no longer be prevented by curative treatment. METHODS: Wistar rats were infected with 600 embryonated eggs of C. hepatica administered by gavage and treated with ivermectin and mebendazole in separate groups at PIDs 10, 12, 15, 17 or 20. Rats from each group and their nontreated controls, were killed and examined 40 days after the end of treatment. RESULTS: Findings by PID 15 were compatible with the stage of complete maturation of infection, when worms and eggs were fully developed and a complex host-parasite multifocal necroinflammatory reaction showed greater intensity, but with no signs of septal fibrosis, which appeared from PID 17 onward. CONCLUSIONS: Since the worms spontaneously died by PID 15, not only septal fibrosis production, but also its maintenance and further development appeared dependent on the presence of eggs, which were the only parasitic factor remaining thereafter.

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Angiogenesis and experimental hepatic fibrosis
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Lemos, Queli Teixeira

; Andrade, Zilton A

Memórias do Instituto Oswaldo Cruz

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Ago 2010, Volume 105 Nº 5 Páginas 611 - 614

Resumo: En | Texto: En | PDF: En

Angiogenesis is a basic change occurring during repair by granulation tissue. This process seems to precede fibrosis formation in most types of chronic liver disease. To examine its presence and significance in different types of hepatic insults, this paper sought to identify the presence, evolution and peculiarities of angiogenesis in the most common experimental models of hepatic fibrosis. The characterization of cells, vessels and extracellular matrix and the identification of factors associated with endothelium (factor VIII RA), vascular basement membrane, other components of the vascular walls (actin, elastin) and the presence of the vascular-endothelial growth factor were investigated. The models examined included Capillaria hepatica septal fibrosis, whole pig serum injections, carbon tetrachloride administration, main bile duct ligation and Schistosoma mansoni infection. The first four models were performed in rats, while the last used mice. All models studied exhibited prominent angiogenesis. The most evident relationship between angiogenesis and fibrosis occurred with the C. hepatica model due to circumstances to be discussed. Special attention was paid to the presence of pericytes and to their tendency to become detached from the vascular wall and be transformed into myofibroblasts, which is a sequence of events that explains the decisive role angiogenesis plays in fibrosis.

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Imaging techniques and histology in the evaluation of liver fibrosis in hepatosplenic schistosomiasis mansoni in Brazil: a comparative study
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Voieta, Izabela

; Queiroz, Leonardo C de

; Andrade, Luciene M

; Silva, Luciana Cristina S

; Fontes, Vitor F

; Barbosa Jr, Aryon

; Resende, Vivian

; Petroianu, Andy

; Andrade, Zilton

; Antunes, Carlos Mauricio

; Lambertucci, José Roberto

Memórias do Instituto Oswaldo Cruz

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Jul 2010, Volume 105 Nº 4 Páginas 414 - 421

Resumo: En | Texto: En | PDF: En

Few publications have compared ultrasound (US) to histology in diagnosing schistosomiasis-induced liver fibrosis (LF); none has used magnetic resonance (MR). The aim of this study was to evaluate schistosomal LF using these three methods. Fourteen patients with hepatosplenic schistosomiasis admitted to hospital for surgical treatment of variceal bleeding were investigated. They were submitted to upper digestive endoscopy, US, MR and wedge liver biopsy. The World Health Organization protocol for US in schistosomiasis was used. Hepatic fibrosis was classified as absent, slight, moderate or intense. Histology and MR confirmed Symmers' fibrosis in all cases. US failed to detect it in one patient. Moderate agreement was found comparing US to MR; poor agreement was found when US or MR were compared to histology. Re-classifying LF as only slight or intense created moderate agreement between imaging techniques and histology. Histomorphometry did not separate slight from intense LF. Two patients with advanced hepatosplenic schistosomiasis presented slight LF. Our data suggest that the presence of the characteristic periportal fibrosis, diagnosed by US, MR or histology, associated with a sign of portal hypertension, defines the severity of the disease. We conclude that imaging techniques are reliable to define the presence of LF but fail in grading its intensity.

20579 downloads Citado 8 vezes em SciELO

Angiogenesis and schistosomiasis
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Andrade, Zilton A

; Santana, Thaynã Souto

Memórias do Instituto Oswaldo Cruz

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Jul 2010, Volume 105 Nº 4 Páginas 436 - 439

Resumo: En | Texto: En | PDF: En

Angiogenesis has been recognised as a precursor of fibrosis in several pathologic conditions. Its participation has been demonstrated in schistosomiasis, both during periovular granuloma formation and in the genesis of schistosomal periportal fibrosis. Paradoxically, proliferation of new blood vessels, accompanied by production of vascular-endothelial growth factor, appeared prominent during fibrosis regression months after curative treatment of schistosomiasis. Thus, angiogenesis in schistosomiasis seems to have a two-way mode of action, participating both in fibrogenesis and in fibrosis degradation. Morphological observations presented here are in keeping with the possibility that, in the first case, angiogenesis allows pericytes to come in great numbers to the site of lesions and be detached from capillary walls and transformed into myofibroblasts, which are important extra-cellular matrix forming cells. During post-curative fibrosis regression, actin-containing pericytes appeared at various foci of tissue remodelling, especially at sites of repair of vascular lesions. The molecular and cell factors involved in both situations seem to be important subjects in need of further investigations and the schistosomiasis model certainly will be of great avail in this regard.

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10.

In vitro and in vivo experimental models for drug screening and development for Chagas disease
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Romanha, Alvaro José

; Castro, Solange Lisboa de

; Soeiro, Maria de Nazaré Correia

; Lannes-Vieira, Joseli

; Ribeiro, Isabela

; Talvani, André

; Bourdin, Bernadette

; Blum, Bethania

; Olivieri, Bianca

; Zani, Carlos

; Spadafora, Carmenza

; Chiari, Egler

; Chatelain, Eric

; Chaves, Gabriela

; Calzada, José Eduardo

; Bustamante, Juan Manuel

; Freitas-Junior, Lucio H

; Romero, Luz I

; Bahia, Maria Terezinha

; Lotrowska, Michel

; Soares, Milena

; Andrade, Sonia Gumes

; Armstrong, Tanya

; Degrave, Wim

; Andrade, Zilton de Araújo

Memórias do Instituto Oswaldo Cruz

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Mar 2010, Volume 105 Nº 2 Páginas 233 - 238

Resumo: En | Texto: En | PDF: En

Chagas disease, a neglected illness, affects nearly 12-14 million people in endemic areas of Latin America. Although the occurrence of acute cases sharply has declined due to Southern Cone Initiative efforts to control vector transmission, there still remain serious challenges, including the maintenance of sustainable public policies for Chagas disease control and the urgent need for better drugs to treat chagasic patients. Since the introduction of benznidazole and nifurtimox approximately 40 years ago, many natural and synthetic compounds have been assayed against Trypanosoma cruzi, yet only a few compounds have advanced to clinical trials. This reflects, at least in part, the lack of consensus regarding appropriate in vitro and in vivo screening protocols as well as the lack of biomarkers for treating parasitaemia. The development of more effective drugs requires (i) the identification and validation of parasite targets, (ii) compounds to be screened against the targets or the whole parasite and (iii) a panel of minimum standardised procedures to advance leading compounds to clinical trials. This third aim was the topic of the workshop entitled Experimental Models in Drug Screening and Development for Chagas Disease, held in Rio de Janeiro, Brazil, on the 25th and 26th of November 2008 by the Fiocruz Program for Research and Technological Development on Chagas Disease and Drugs for Neglected Diseases Initiative. During the meeting, the minimum steps, requirements and decision gates for the determination of the efficacy of novel drugs for T. cruzi control were evaluated by interdisciplinary experts and an in vitro and in vivo flowchart was designed to serve as a general and standardised protocol for screening potential drugs for the treatment of Chagas disease.

12866 downloads Citado 9 vezes em SciELO

11.

Pulmonary changes during acute experimental murine manson schistosomiasis
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Souza, Samaly dos Santos

; Souza Neto, Joaquim Pereira de

; Andrade, Zilton A.

Revista da Sociedade Brasileira de Medicina Tropical

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Fev 2009, Volume 42 Nº 1 Páginas 5 - 8

Resumo: Pt En | Texto: Pt En | PDF: Pt | PDF: En

Recentemente tem sido observada a presença de tosse seca, dispnéia, e manifestações de asma brônquica em pacientes com esquistossomose aguda. Para se investigar sobre o tipo e patogenia de tais lesões foi utilizado um modelo experimental de esquistossomose aguda no camundongo. Quarenta animais foram divididos em quatro grupos de 10 animais cada, 3 infectados e um grupo controle não-infectados. Os exames foram feitos após 7, 28-35, e 40 dias após a exposição cercariana. Na fase aguda da infecção (28-35 dias), encontrou-se um processo de pneumonite intersticial multifocal, envolvendo os tecidos peribrônquicos, peribronquiolares e subpleural, processo que esteve ausente nas outras fases examinadas. Não foi possível a demonstração de antígenos do Schistosoma. mansoni nas lesões da fase aguda, através da técnica de imuno-fluorescência indireta. A pneumonite foi atribuída a produtos (mediadores inflamatórios) gerados nas lesões hepáticas necro-inflamatórias periovulares da fase aguda, e transportados para os pulmões pela circulação sanguínea.

Dry cough, dyspnea and manifestations of bronchial asthma have recently been observed in patients with acute schistosomiasis. To investigate the type and pathogenesis of these conditions, an experimental mouse model for acute schistosomiasis was used. Forty mice were divided into four groups of ten each: three infected groups and a non-infected control group. The animals were examined 7, 28-35 and 40 days after exposure to cercariae. During the acute phase of the infection (28-35 days), a process of multifocal interstitial pneumonitis involving the peribronchial, peribronchiolar and subpleural tissues was found. This process was not seen during the other phases of the infection. Indirect immunofluorescence failed to demonstrate the presence of schistosomal antigens in the acute-phase lesions. The pneumonitis was attributed to products (inflammatory mediators) from acute-phase periovular necrotic-inflammatory lesions in the liver that were transported to the lungs by the bloodstream.

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12.

Frações de fósforo em solo adubado com fosfatos em diferentes modos de aplicação e cultivado com milho
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Santos, José Zilton Lopes

; Furtini Neto, Antonio Eduardo

; Resende, Álvaro Vilela de

; Curi, Nilton

; Carneiro, Leandro Flávio

; Costa, Sérgio Ely Valadão Gigante de Andrade

Revista Brasileira de Ciência do Solo

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Abr 2008, Volume 32 Nº 2 Páginas 705 - 714

Resumo: Pt En | Texto: Pt En | PDF: Pt | PDF: En

O histórico de uso e o manejo da adubação influenciam a capacidade de suprimento de P pelo solo. Neste trabalho, foram avaliadas as frações de P num Argissolo Vermelho da região do Cerrado, adubado com fosfatos de reatividade distinta, em diferentes modos de aplicação e cultivado com milho durante três safras. A área, que já havia sido adubada em épocas passadas, estava coberta por braquiária. O delineamento experimental foi o de blocos casualizados com quatro repetições, num esquema fatorial 4 x 3 + 1, envolvendo quatro fontes de P, na quantidade de 180 kg ha-1 de P2O5 (superfosfato triplo, termofosfato magnesiano, fosfato natural reativo de Arad e fosfato natural de Araxá), três formas de aplicação (a lanço em área total no primeiro ano, localizada no sulco de plantio no primeiro ano e parcelada anualmente no sulco) e uma testemunha (sem P) como tratamento adicional. O P foi fornecido considerando-se os teores totais do nutriente nas fontes. Após três cultivos de milho, foram retiradas amostras de solo na profundidade de 0-20 cm para o fracionamento do P. A interação entre fontes e modos de aplicação de P interfere nas frações do nutriente no solo no final do cultivo de milho. De modo geral, o parcelamento da adubação condiciona maior teor do nutriente nas frações inorgânica (todas as fontes) e orgânica (fontes mais reativas). O fato de a área ter sido anteriormente adubada e ocupada por braquiária influenciou os efeitos dos tratamentos, pois a produção de milho foi relativamente elevada onde não houve aplicação de P. Houve evidências da participação de frações consideradas pouco lábeis no suprimento de P para o milho, em função da diminuição dessas frações no solo.

The land use history and management of fertilization influence the soil phosphorus supply capacity. In this study, the P fractions in a Red Argisol (Ultissol) of the cerrado region were evaluated under different application methods and with phosphorus sources of different solubility, after three successive corn crops. The area had already been fertilized and cultivated in the past and remained covered with Brachiaria grass. A randomized block design with four replications was used, in a 4 x 3 + 1 factorial scheme, involving four P sources at a rate of 180 kg ha-1 P2O5 (triple superphosphate, magnesium thermophosphate, Arad reactive rock phosphate, and Araxá rock phosphate), three application methods (broadcasted in the first year, in-furrow application in the first year, and annually in-furrow split applications), and a control plot (without P) as additional treatment. The applied P rate was based on the total P2O5 content of each fertilizer. After three corn cropping seasons, soil samples were collected at a depth of 0-20 cm to determine the P fractions. The interaction between P sources and application methods interferes with the P fractions in the soil towards the end of the growing season. In general, split fertilization resulted in a higher values of inorganic (all sources) and organic P fractions (soluble sources). The fact that the area had previously been fertilized and cultivated with Brachiaria grass influenced the treatment effects, as shown by the relatively high crop yield of the control treatment not fertilized with P. There are evidences for the participation of less-labile P fractions in P supply to corn due to the observed reduction of these fractions in the soil.

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13.

Thalidomide failed to inhibit angiogenesis and fibrosis in hepatic schistosomiasis of the mouse
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Lima, Camila Bião

; Iglesias, Karen Brasil

; Andrade, Zilton A

Memórias do Instituto Oswaldo Cruz

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Nov 2007, Volume 102 Nº 7 Páginas 883 - 885

Resumo: En | Texto: En | PDF: En

The relationship between angiogenesis and fibrosis has been demonstrated in several pathological conditions, one of them being schistosomiasis. To observe whether suppression of angiogenesis would interfere with fibrosis, Thalidomide, an anti-angiogenesis drug, was administered during 30 consecutive days to mice with experimental schistosomiasis. Computerized morphometric measurements of fibrosis, and the counting of blood vessels from hepatic schistosomal lesions did not significantly differ when treated animals and their controls were compared at the end of the experiments. These rather unexpected results are presented under the understanding that they may be of interest during further studies on the anti-angiogenesis properties of thalidomide, and the relationship between angiogenesis and fibrosis.

1678 downloads Citado 1 vez em SciELO

14.

Role of partial hepatectomy on Capillaria hepatica-induced hepatic fibrosis in rats
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Santos, Carolina Cincurá Silva

; Onofre-Nunes, Záira

; Andrade, Zilton Araujo

Revista da Sociedade Brasileira de Medicina Tropical

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Out 2007, Volume 40 Nº 5 Páginas 495 - 498

Resumo: Pt En | Texto: Pt En | PDF: Pt | PDF: En

Sabe-se que a fibrose hepática pode sofrer uma redução em seqüência uma hepatectomia parcial, uma vez que o parênquima hepático se regenera muito rápido, mas não o excesso de tecido fibroso. O presente trabalho avalia esta hipótese ao observar como se comporta a fibrose septal sistematizada induzida pela Capillaria hepática no rato, após infecção de 30 ou 90 dias de duração, em animais submetidos à hepatectomia parcial. Os resultados revelaram que a fibrose em si mesma não foi afetada na sua morfologia, mas a sua quantidade relativa apareceu diminuída significativamente no campo microscópico como conseqüência do aumento da massa de tecido hepático pós-regeneração.

It is known that hepatic fibrosis may regress following partial hepatectomy, since the hepatic parenchyma regenerates very rapidly, but not the excess of fibrous tissue. The present study evaluated this hypothesis by observing the behavior of systematized septal fibrosis induced by either 30 or 90-day-old Capillaria hepatica infection, in rats subjected to partial hepatectomy. The results revealed that the morphology of the fibrosis was unaffected, but its relative quantity within the microscope field appeared significantly decreased, as a consequence of the increased liver tissue mass following regeneration.

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15.

Ki-67 is expressed in multiplying forms of Schistosoma mansoni, but not in snail host tissues
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Silva, Tânia Maria Correia

; Souza, Samaly dos Santos

; Almeida, Tais Fontoura de

; Andrade, Zilton A

Memórias do Instituto Oswaldo Cruz

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Ago 2007, Volume 102 Nº 5 Páginas 651 - 653

Resumo: En | Texto: En | PDF: En

Ki-67 is a protein expressed in the nucleus of several species during cell-division, being absent during the GO resting phase of the cellular cycle. During attempts to disclose mitosis in the so-called " amebocyte-producing organ " in Biomphalaria glabrata infected with Schistosoma mansoni, the parasite multiplying forms appeared strongly marked for Ki-67, while the snail tissues were completely negative. These data are worth registering to complement general data on Ki-67, and to help future studies on the relationship of the parasite and of its intermediate host.

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